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Generating a model of the three-dimensional spatial distribution of neurons using density maps.

机译:使用密度图生成神经元的三维空间分布模型。

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Microcolumns are a vertical arrangement of neocortical neurons that may constitute a fundamental computational ensemble but have been difficult to study morphologically because of the challenges of determining the three-dimensional (3D) spatial arrangements of individual neurons in the ensemble. Previously, a statistical density map method was developed to characterize microcolumns using two-dimensional (2D) coordinates of neurons from thin tissue sections. Here we extend this approach to derive the relationship between these 2D density maps and the actual 3D properties of microcolumns by creating a theoretical 3D model of cortical neurons. In seven steps, we transform a 3D initial arrangement of neurons from a crystalline lattice, with distances and neuron numbers approximating the idealized cortical microcolumn as assayed by our 2D density map analysis, into a model whose neuronal locations represent a plausible 3D arrangement of neurons in the brain. Because we constrain the transformations on the 3D model by the 2D density map properties, the transformed 3D model will exhibit properties that are consistent with experimental findings regarding microcolumnar anatomy in the brain. Moreover, because our methodology only requires the x,y locations of neurons from thin sections, it is readily accessible to any set of input data regardless of preparation or staining, from human or animals. By generating 3D model neuronal arrangements and comparing between control, aged, and diseased brain, our method can be used to test hypotheses about the effects of neurological diseases as well as normal aging on the 3D structure of microcolumns in the brain.
机译:微柱是新皮层神经元的垂直排列,可能构成基本的计算集合,但由于确定集合中单个神经元的三维(3D)空间排列的挑战而很难进行形态学研究。以前,已开发出一种统计密度图方法来使用来自薄组织切片的神经元的二维(2D)坐标来表征微柱。在这里,我们通过创建皮层神经元的理论3D模型来扩展此方法,以导出这些2D密度图与微柱的实际3D属性之间的关系。在7个步骤中,我们将一个2D密度图分析所测定的神经元的3D初始排列从晶格转换为一个模型,该距离和神经元数目近似于理想的皮层微柱(通过2D密度图分析测得),该模型的神经元位置代表了3D神经元的合理3D排列大脑。因为我们通过2D密度图属性限制了3D模型上的转换,所以转换后的3D模型将显示与关于大脑微柱解剖的实验结果相一致的属性。此外,由于我们的方法仅需要薄切片中神经元的x,y位置,因此,无论来自人或动物的准备或染色情况如何,任何输入数据集都可以轻松访问它。通过生成3D模型神经元排列并在对照,老年和患病的大脑之间进行比较,我们的方法可用于测试有关神经系统疾病以及正常衰老对大脑微柱3D结构的影响的假设。

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